Philips recently announced that it is voluntarily recalling approximately 5,400 HeartStart FR2+ automated external defibrillators (AEDs). This recall is being conducted due to the possibility of a ...
The U.S. Food and Drug Administration has issued a safety communication saying certain HeartStart automated external defibrillator devices made by Philips Medical Systems, a division of Philips ...
The Food and Drug Administration (FDA) is warning consumers that some models of HeartStart automated external defibrillators (AED) may not work during a cardiac emergency. The devices, which are made ...
HealthDay News — The FDA is advising owners of Philips HeartStart automated external defibrillator (AED) devices to contact the company to ascertain whether their device is among those that might be ...
Philips is parting ways with its worldwide emergency care business, including its catalog of automated external defibrillators and other hardware used inside and outside the hospital, through a ...
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